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7.2 years ago
tarek.mohamed
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370
Hi All,
I have two final illumina reports from bead chip experiment (300,000 SNPs). Ideally genotypes of these two samples should be identical. How can I compare between the genotypes of the two samples to see if they are really identical or there are some mismatches?
The files look like this;
CHROM POS ID Sample_ID Allele1 Allele2 GC_Score
3 183635768 rs1000002 200638550003_R01C01 A G 0.8902
3 98342907 rs1000003 200638550003_R01C01 A G 0.9351
4 103374154 rs10000030 200638550003_R01C01 A G 0.7764
4 38924330 rs10000037 200638550003_R01C01 G G 0.929
4 165621955 rs10000041 200638550003_R01C01 A A 0.8957
2 237752054 rs1000007 200638550003_R01C01 A G 0.9491
Thanks Tarek
Hi Kronenberg, Thanks for the reply! What would be the best way to convert illumina genotype report to VCF?
Regards Tarek